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br Heteroplasmy mitochondrial segregation and disease
2018-10-24
Heteroplasmy, mitochondrial segregation and disease In an individual with a mitochondrial disease, different cells or populations may have differing amounts of the mutant mitochondria, ranging from complete homoplasmy – individuals with all mutant mitochondrial DNA as occurs in Leigh\'s Syndrome
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The neurogenic to gliogenic transition of NSPCs is
2018-10-24
The neurogenic-to-gliogenic transition of NSPCs is probably governed by a multi-layered system. The epigenetic status of astrocyte-specific (Takizawa et al., 2001) and neurogenic genes changes during development (Hirabayashi et al., 2009; Kishi et al., 2012; Pereira et al., 2010), critically determi
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All PGCs differentiated from ESCs in our study
2018-10-24
All PGCs differentiated from ESCs in our study, regardless of differentiation approach or sorting strategy, were capable of implementing ICC erasure at the Snprn ICC. However, unlike E9.5 PGCs from the embryo, the hypomethylated state at this ICC was unstable, and in every case re-methylation was in
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Many SMs have been reported to facilitate reprogramming
2018-10-24
Many SMs have been reported to facilitate reprogramming. For example, sodium butyrate (N, NaB), a histone deacetylase (HDAC) inhibitor, greatly improved reprogramming efficiency by upregulating epigenetic remodeling and pluripotency-associated fasudil (Mali et al., 2010; Zhang and Wu, 2013). In anot
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dna-pkcs br Results br Discussion In this
2018-10-24
Results Discussion In this study we have shown that activating BRAF mutations leading to increased RAS/MAPK pathway signaling induce a hypertrophic phenotype in hiPSC-derived CMs. While BRAF-mutant CMs display intrinsic defects in Ca2+ handling, several aspects of their phenotype require parac
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IGF and PI K signaling in regenerating muscle was tightly
2018-10-24
IGF and PI3K signaling in regenerating muscle was tightly regulated across multiple levels and temporally, especially during the transition between myoblast proliferation and differentiation. In the early period, IGF1 was upregulated and quickly followed by increases in expression and chromatin remo
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br Experimental Procedures br Author Contributions br
2018-10-24
Experimental Procedures Author Contributions Acknowledgments This work is supported by national Portuguese funding through FCT, Fundação para a Ciência e a Tecnologia, project UID/BIM/04773/2013 CBMR, projects PEst-OE/EQB/LA0023/2013 and PTDC/SAU-ENB/111702/2009 to J.B., U01HL100408, NIH/NH
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Mosaicism in CGG repeat length is
2018-10-24
Mosaicism in CGG repeat length is often observed in FXS patients, who carry both premutation and full mutation atp citrate lyase inhibitor and therefore differ in the proportion of cells with silenced FMR1, which contributes to the clinical spectrum of FXS phenotypes (Rousseau et al., 1994). Mosaic
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Epigenetic modification by active DNA demethylation
2018-10-24
Epigenetic modification by active DNA demethylation or histone demethylation has been shown to facilitate iPSC induction in human and mouse (Huangfu et al., 2008a, 2008b). Tet1, a DNA methylcytosine dioxygenase, can facilitate iPSC induction by promoting Oct4 demethylation and re-activation, and eve
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This however does not take place An insignificant
2018-10-24
This, however, does not take place. An insignificant decrease in the and ΔEv values in n-PbS : O+ compared to the data for the initial sample is within the margin of experimental error and could be regarded merely as a tendency in value decrease of the energy parameters discussed when passing from
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br Numerical computations We present here the calculation da
2018-10-24
Numerical computations We present here the calculation data obtained for the structure prepared from ytterbium (Yb, eφ = 3.1 eV) and carbon (C, eφ = 4.7 eV) layers. Calculations necessary to optimize the layered field emitters and determine their emission characteristics have been carried out us
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NSC23766 The shape and the location
2018-10-24
The shape and the location of this peak were examined, and the parameters necessary for constructing the Fano profile (6) were computed (see Table 2). The computed peak location is in good agreement with the experiment; unfortunately, however, since it is narrow and highly intense, no specific conc
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When the parameter is close
2018-10-24
When the parameter μ is close to zero, we will have: From here it follows that in the case of a low relative hardness of the composite, the SIF limit values are expressed by formulae (29) for a homogeneous wedge at . Notice that asymptotes (31) and (32) can also be obtained by solving the limitin
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In this contribution we treat the growth
2018-10-24
In this contribution, we treat the growth of fullerenes as a series of joining reactions of cupola half-fullerenes C10, C12, C16, C20, and C24[9] through the use of the geometrical modeling. Reaction between two base-truncated triangular pyramids The atomic configurations corresponding to reacti
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or instead of formulas in the case of polynomials of
2018-10-24
or instead of formulas in the case of polynomials of arbitrary degree of homogeneity k or m[15]. The final results are given below; there are configurations that differ greatly compared with the common formulas presented in Ref. [15]. Potentials which are symmetrical with respect to z and with e
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